化学
光敏剂
光热治疗
苯并噻唑
光动力疗法
部分
活性氧
癌症研究
荧光
生物物理学
衍生工具(金融)
组合化学
癌细胞
细胞凋亡
DNA
转移
单线态氧
肿瘤细胞
赫拉
生物化学
线粒体
联合疗法
癌症
细胞生长
癌症治疗
纳米颗粒
细胞
体外
立体化学
DNA损伤
细胞周期检查点
细胞培养
细胞毒性
癌症治疗
结构-活动关系
肿瘤进展
作者
Jiapeng Dong,Hongshan Xie,Guining Cao,Jiacheng Tang,Xiaofeng Li,Qitong Qin,Ziqiao Li,Zhenxing Pan,Yaoxun Zeng,Xiang Su,Xinlu Fu,Yan He,Liu Xujie
标识
DOI:10.1021/acs.jmedchem.5c03244
摘要
Mitochondrial DNA G-quadruplexes (mtDNA G4s) are promising therapeutic targets for cancer, driving the need for innovative theranostic agents. We report SPNO, a mitochondria-targeted near-infrared (NIR) hemicyanine derivative that integrates triple-modal functions: fluorescence imaging, G4 stabilization, and synergistic phototherapy. SPNO incorporates a triphenylphosphonium targeting moiety and a modified benzothiazole core with methoxy substitution and an extended π-bridge, enabling NIR absorption/emission and real-time tumor localization. It selectively binds and stabilizes mtDNA G4s, inducing G0 and G1 cell cycle arrest and metastasis inhibition. Under 685 nm laser irradiation, SPNO generates type I and II reactive oxygen species (ROS) with efficient photothermal conversion, achieving combined photodynamic therapy (PDT) and photothermal therapy (PTT). Unirradiated SPNO intrinsically suppresses tumor growth via G4 stabilization. In vivo, SPNO-mediated theranostics significantly inhibited breast tumors without systemic toxicity, showcasing a novel strategy for precision cancer treatment.
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